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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265197Generated: October 25, 2026

2,1,3-Benzothiadiazole, 4-chlorosulfonyl- → 2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4,5-dichloro-benzoic acid methyl ester

https://huagongshe.com/reaction/2265197

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,1,3-Benzothiadiazole, 4-chlorosulfonyl-HCID 2735459—
ReactantMethyl 2-amino-4,5-dichlorobenzoateHCID 11694243—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Product2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4,5-dichloro-benzoic acid methyl esterHCID 6877054350%

Reaction Steps

The title compound (0.95 g, 50%) was prepared from methyl 2-amino-4,5-dichlorobenzoate and 4-chlorosulfonyl-2,1,3-benzothiadiazole as in Example 1, Part A (without DMAP). 1H NMR (500 MHz, CDCl3): 11.21 (s, 1H), 8.39 (dd, J=7.1, 1.0, 1H), 8.25 (dd, J=8.8, 1.0, 1H), 7.94 (s, 1H), 7.91 (s, 1H), 7.74 (dd, J=8.8, 7.1, 1H), 3.93 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855292B2
Source datasetuspto-grants-2010_12
ORD IDord-d9fbe2007c7d42e192abe7170acdb79c
Source noteuspto-grants-2010_12